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	<title>Housefly (Musca domestica L.)-borne multidrug resistant enteric bacteria in Nigerian urban abattoirs and their spread in surrounding built environment - Microbiology Archives, an International Journal</title>
	<link>https://microjournal.researchfloor.org/housefly-musca-domestica-l-borne-multidrug-resistant-enteric-bacteria-in-nigerian-urban-abattoirs-and-their-spread-in-surrounding-built-environment/</link>
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                        <title>Housefly (Musca domestica L.)-borne multidrug resistant enteric bacteria in Nigerian urban abattoirs and their spread in surrounding built environment</title>
                        <link>https://microjournal.researchfloor.org/housefly-musca-domestica-l-borne-multidrug-resistant-enteric-bacteria-in-nigerian-urban-abattoirs-and-their-spread-in-surrounding-built-environment/</link>
                        <pubDate>Mon, 26 May 2025 04:04:00 +0000</pubDate>
                        <dc:creator>admin</dc:creator>
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                        <guid isPermaLink="false">https://microjournal.researchfloor.org/?p=2364</guid>
                        <abstract language="eng"><p>Houseflies (<em>Musca domestica</em> L.) are known carriers of infectious agents which may include multidrug-resistant (MDR) pathogenic bacteria. Thus the prevalence and antibiotic resistance profiles of housefly-borne enteric bacteria in 16 Nigerian urban-based abattoirs and their dispersal in built environment surrounding the abattoirs were investigated. The insect-baiting technique was used to capture 1600 houseflies in the abattoirs and surrounding residential/commercial buildings’ outdoor environments. Enteric bacteria were isolated from the flies using selective and differential media, and they were identified by cultural and biochemical characteristics. Antibiotics resistance of these bacteria was ascertained by agar diffusion technique using 15 antibiotics. The identified isolates were <em>Escherichia coli</em>, <em>Salmonella</em> <em>enterica</em>, <em>Shigella</em> <em>dysentariae</em> and <em>Klebsiella pneumonia</em> with prevalence variations of 4.3-7.3% and 4.5-7.4% in abattoirs and buildings’ outdoor environment, respectively. The enteric bacteria populations from abattoirs to buildings did not correlate with distance (r=0.03-0.10; <em>P</em>&gt;0.05); and no significant inter-bacterial correlation in dispersals was found except between <em>S. enterica</em> and <em>S. dysentariae</em> (r=0.65; <em>P</em>=0.006). All the isolates were susceptible to ceftriaxone and gentamycin, while varied resistance and susceptibility was observed with respect to other antibiotics. The isolates were mostly MDR with multiple antibiotics resistant index of 0.50-0.78 without significant difference between isolates from the abattoir and buildings’ outdoor houseflies. Compared to building outdoors, MDR isolates from abattoir houseflies were significantly more in number (<em>P</em>=0.000-0.015) in over 65% of the abattoir locations. These findings can be an impetus for the intervention of public health agencies in abattoir operations to control the dispersal of MDR bacteria in built environment.</p>
</abstract>
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<p><strong>1.0 INTRODUCTION</strong></p>



<p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Buildings and other structures where animals are slaughtered and prepared for human consumption are generally known as abattoirs [1]&nbsp;and they have consistently been a source of major concern to public health professionals and environmentalists because of the wastes generated. Abattoirs have been recognized as a critical link in spreading pathogenic bacteria to the environment [2, 3]; and this includes enteric bacteria which may be multidrug-resistant (MDR).&nbsp; Indeed, MDR enteric bacteria such as&nbsp;<em>E. coli</em>,&nbsp;<em>Salmonella</em>, and&nbsp;<em>Shigella</em>&nbsp;spp. have been isolated in abattoir settings [4].</p>



<p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Wastes generated by abattoirs usually attract houseflies, which feed, breed, and lay numerous eggs on the animal wastes and nearby rotten organic matter [5, 6]. Houseflies (<em>Musca domestica</em>&nbsp;L.) are generally known to be associated with man and his activities [7]. Eateries, markets, kitchens, hospital environment, and poultries are typical examples of places where flies are found in abundance and can potentially become vectors of diseases [8]. Houseflies hop from one substrate to another in the course of feeding and the substrates may contain pathogenic bacteria thereby making them vectors of pathogenic bacteria [9, 10]. It is therefore obvious that the presence of houseflies in abattoirs can portend danger in the context of public health management; and this should be worrisome. [11-14].</p>



<p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Several reports have shown that infectious microorganisms have been transmitted to humans by houseflies from various sources. The type of infectious agent is dependent on the source of the carrier-housefly hence flies captured from sites where the use of antibiotics is common (e.g. hospital and agricultural settings) bear antimicrobial-resistant bacteria and fungi [11, 15-19]. In addition, there are indications that nosocomial infections are transmissible by houseflies present in the hospital environment [15, 20] while housefly-borne strains of virulent microorganisms and antibiotic-resistant genes can also be dispersed in the same environment [21, 22]. The potential risk of the spread of housefly-borne MDR bacteria from agricultural, clinical and domestic settings should be of public health concern. &nbsp; Abattoirs generate enormous effluents which can become potential “hot zones” for gene pools that may ultimately culminate in the emergence of MDR organisms [23]. Reports have shown that antibiotic-resistant bacteria abound in abattoir environments [24-26], with <em>Salmonella</em>&nbsp;[25], entero-hemorrhagic&nbsp;<em>E</em>.&nbsp;<em>coli</em>&nbsp;(EHEC) 0157:H7 [27] and methicillin-resistant&nbsp;<em>S</em>.&nbsp;<em>aureus</em>&nbsp;[28] as typical examples among others.</p>



<p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Abattoirs in many urban areas of Nigeria are often located close to residential and commercial buildings or human settlements grow to meet the abattoirs. While it has been established that abattoirs’ effluents contain pathogenic and MDR bacteria, there is a paucity of information on the role of flies in spreading pathogens from abattoirs in built environments in urban settings. Thus the study was designed to: 1, determine the presence of MDR enteric bacteria on houseflies in abattoirs located in urban built environment; and 2, ascertain the spread of MDR enteric bacteria to surrounding buildings by the houseflies. The outcome of the investigation may prove useful for public health control measures.</p>



<p><strong>2.0 Materials and Methods</strong></p>



<p>2.1 <em>Abattoir location and sample </em><em>collection</em></p>



<p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Abattoirs and environments located in four urban areas (Warri, Abraka, Obiaruku and Kwale towns) in Delta State, Nigeria were selected for the investigation. Abattoirs close to residential and commercial areas were investigated and 16 at 4 per town were selected for the study..</p>



<p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Adult houseflies were captured from the selected abattoirs and surrounding buildings’ outdoors (0-100m) using insect-baited trap [29]. The flies were collected over a period of six months at 100 per location bringing it to a total of 1,600. They were subsequently placed in zip-locked polythene bags and taken to the laboratory and killed by storage in refrigerator at -20 <sup>o</sup>C [30]. Thereafter, they were singularly stored in 2 mL sterile NaCl (0.85% w/v) in tubes at 4°C till needed for subsequent tests.</p>



<p><em>2.2 Isolation </em><em>and identification of housefly-borne enteric bacteria</em><em></em></p>



<p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Houseflies weighing 1 g was placed in 9 ml of sterile phosphate-buffered saline (PBS) and shaken manually to dislodge the bacteria on the flies. Aliquots of the dilutions were used to inoculate MacConkey agar, <em>Salmonella-Shigella</em> agar, and Eosine Methylene Blue agar all Oxoid, Basingstoke). Incubation of plates was at 37<sup>o</sup>C for 24-48h and distinct colonies were sub-cultured and stored for identification.&nbsp; Representative colonies (5/plate) were selected and subjected to biochemical tests for confirmation of their identities. The biochemical tests carried out include indole, methyl red, catalase, Voges-Proskauer, citrate utilization, triple sugar iron agar (TSI), motility, urease, L-lysine decarboxylase, L-ornithine decarboxylase, sodium acetate and Christensen’s citrate test. Fermentation tests using dulcitol, glucose, lactose, mannitol, raffinose, salicin, sorbitol, sucrose and xylose, (Oxoid, UK), were also carried out. The Analytical Profile Index (API) system (Liofilchem, Italy) was used to confirm the outcome of the cultural and biochemical identification tests.</p>



<p><em>2.3 Antibiotics </em><em>susceptibility test</em></p>



<p>Antibiotic susceptibility test was conducted by the disk diffusion method using Mueller-Hinton agar (Oxoid, UK) following CLSI [31] standards. The antibiotics used were: Cefotaxime, 30μg; Tetracycline, 30 μg; Ceftriaxone, 30μg; Piperacillin, 20μg; Ampicillin, 20μg; Cefoxitin, 30 μg; Cotrimazole, 30 μg; Gentamycin, 30μg; Ciprofloxacin, 30μg; Levofloxacin, 30μg; Ofloxacin, 30μg; Chloramphenicol, 20μg; Azythromycin, 20μg; Imempenem, 20μg; and Vancomycin, 20μg. The plates were incubated for 18-24h at 37°C before the zones of clearance (inhibition) were measured.</p>



<p><em>2.4 Data analysis</em></p>



<p>Determination of multiple antibiotics resistance (MAR) index was by dividing the number of antibiotics resisted by the total number of antibiotics used. Bacteria isolates with MAR index ≥0.3 was by convention taken as multidrug-resistant (MDR).. The difference between the MAR index of the enteric bacteria isolated from houseflies in abattoirs and surrounding buildings was analyzed by <em>t</em>-test. A similar comparative analysis was carried out for MDR bacterial population after log<sub>10</sub> transformation. Pearson correlation statistics was used to test the relationship between distances from abattoir and the population of housefly-borne enteric bacteria in the surrounding buildings after log<sub>10</sub> transformation. Correlations within the enteric bacteria were similarly analyzed.</p>



<p><strong>3.0 Results</strong></p>



<p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Table 1 presents information on the features and state of the environment of the 16 abattoirs investigated across 4 towns in Delta State, Nigeria. The expected features of an abattoir were present in all the abattoirs although with some variations. Visual observation showed that the distances of wastewater discharge points, composting sites and bone dumpsites from the slaughter buildings varied (0-30m). The distances of the abattoirs from surrounding commercial and residential buildings also varied (Table 1)</p>



<p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; The number of enteric bacteria isolated from houseflies located in the abattoirs and surrounding buildings’ outdoor environments were 2008 and1252, respectively. The isolates were <em>E. coli, S. enterica S. dysenteriae and K. pneumonia </em>irrespective of locations and sites of abattoirs (Figure 1). Although not marked, there were variations in the prevalence of the isolates with ranges of: 6.0-6.9 (<em>E. coli</em>); 5.9-7.4, (<em>S. enterica</em>); 4.5-6.7 (<em>S. dysentariae</em>); and 4.3-7.3 (<em>K. pneumonia</em>) as shown in Figure 1 based on the totality of the isolates from all abattoirs and surrounding buildings outdoor environment. Prevalence variations by locations (towns) and differences between abattoirs and surrounding buildings were not markedly different (Figure 1).</p>



<p>Table 1: Features of abattoir environment and distance from residential/commercial buildings</p>



<p>Figure 1:Prevalence <strong>of</strong> housefly-borne enteric bacteria in abattoir and surrounding buildings’ environment by overall assessment</p>



<p><strong>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; </strong>There was no significant correlation between distance from abattoirs and the population of the housefly-borne enteric bacteria in the surrounding buildings’ environment (Table 2). In the context of association within the four enteric bacteria, <em>S. enterica</em> and <em>S dysentariae </em>negatively highly (r=-0.65) correlated (Table 2). A further analysis of Table 2 showed that correlation coefficients were generally very low (≤ 0.10) as it concerns the association between distance and enteric bacterial population in buildings. Although the correlation coefficients were not significant, intra-enteric bacteria correlations were markedly higher (0.14-0.34) when compared to that of distance (Table 2).</p>



<p>Table2: Correlation analyses of the associations within the housefly-borne enteric bacteria population and distance from abattoir to surrounding buildings</p>



<p>*<em>P</em>=0.006</p>



<p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; All the isolates from flies in the abattoir and surrounding buildings’ outdoor environment were susceptible to ceftriaxone and gentamycin, while varied resistance and susceptibility was observed amongst the other antibiotics used (Figures 2-5). In addition, <em>E. coli</em> isolates were susceptible to cefoxitin while strains from houseflies in buildings tended to be more highly resistant to greater number of antibiotics than those from abattoirs (Figure 2). In addition to ceftriaxone and gentamycin, <em>S. enterica</em> from both sources (abattoirs and buildings) were also susceptible to ciprofloxacin (Figure 3). Again, the trend of more high antibiotic resistance from building strains was repeated (Figure 3). Compared to <em>E. coli</em> and <em>S. enterica,</em> there was susceptibility to more antibiotics by <em>S. dysentariae</em> (Figure 4). In contrast to the trends shown in Figures 2 and 3, <em>S. dysentariae</em> strains from abattoirs were more highly resistant to greater number of antibiotics than those from buildings (Figure 4). Isolates of <em>K. pneumonia</em> were generally less resistant to antibiotics with building strains showing greater antibiotic susceptibility (Figure 5)</p>



<p>The MAR index of the enteric bacteria isolates is presented in Table 3. It ranged from 0.5 to 0.78 making them highly multidrug resistant (≥ 0.3). Although differences between isolates from abattoir and surrounding buildings can be seen, statistical analysis by <em>t</em> test did not reveal any significant differences (Table 3).</p>



<p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; A comparison of the population of the housefly-borne MDR isolates in abattoirs and surrounding buildings outdoor environment is presented in Table 4. Except in few cases, the MDR isolates from abattoir houseflies were significantly greater in number than those from surrounding buildings irrespective of the bacteria species.</p>



<p><strong>4.0 Discussion</strong></p>



<p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; An abattoir or slaughterhouse is a premise for slaughtering, processing and practical preservation of animals for human consumption that is usually registered with the appropriate public health agency [32]. Meat cutting table, <a href="https://www.lawinsider.com/dictionary/slaughter-house-abattoirslab">slaughter slab</a>s<strong>, wastewater discharge points, and composting sites are common features of abattoirs that also characterized the abattoirs investigated in this study; and they are potential sources of pathogenic bacteria arising from faecal matter of slaughtered animals [33]. In this study, enteric bacteria were present on the bodies of houseflies captured in all abattoirs as well as the outdoor environments of the surrounding buildings investigated; and they were found to be MDR. Indeed, MDR pathogenic bacteria have been isolated from abattoirs especially the waste water [33]. H</strong>ouseflies become contaminated by bacteria in the course of feeding in the abattoirs and their hopping behavior spreads the bacteria [9, 10]. Houseflies regurgitate food and deposit them on solid food before ingestion in what is known as bubbling; and this regurgitation and their faecal matter is associated with transmission of pathogens [34]. &nbsp;Given this scenario, the presence of enteric bacteria-contaminated houseflies in abattoirs and the surrounding environment would not have been a surprise.</p>



<p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; The finding that there was no marked difference between abattoirs and surrounding buildings in the prevalence of housefly-borne enteric bacteria indicated that the flies migrated from abattoirs. Although houseflies tend to remain in their feeding and breeding localities, they are also known to travel long distances and disperse to residential areas, schools, and business premises [35, 36]. Indeed, dispersal of houseflies at distances greater than 12km has been reported [34]. The dispersal of houseflies may not be unidirectional like a swarm of bees or follow a pattern of reduced population density with distance. Dispersal and distances tend to be influenced by location of feeding sites and deflected wind in built environment hence it may therefore be circuitous [37]. This observation is supported by the absence of a significant correlation between the density of housefly-borne enteric bacteria and distance from abattoirs. The significant negative correlation between <em>S. enterica</em> and <em>S. dysentariae</em> both with the same intestinal ecological niche can be explained by the higher survival rate of <em>Salmonella enterica</em> in the environment. This explanation is supported by the observation that the prevalence of <em>S. enterica</em> in the outdoor environment of buildings was higher than that of <em>S. dysentariae</em> (6.4 <em>vs</em> 5.9%)</p>



<p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; The movement of the flies from abattoirs to the buildings is further indicated by the non-significant difference between the MAR index of the housefly-borne enteric bacteria in abattoirs and surrounding buildings outdoor environment. Similarity in antibiotic resistant profile was indicated by the common susceptibility to gentamycin and ceftriaxone and resistance to five of the antibiotics used. The finding that the number of housefly-borne MDR enteric bacteria in abattoirs exceeded those in buildings does not contradict the dispersal trend. The reason is that flies can remain longer in their abattoir feeding sites and may aggregate in other sites where they find food in the course of migration [34]. It was observed that <em>E. coli</em> and <em>S. enterica</em> on houseflies in the outdoor environment of surrounding buildings exhibited greater antibiotic-resistance when compared to isolates from abattoir-based flies while it was the opposite for <em>S. dysentariae</em> and <em>K. Pneumonia</em>. This seemingly inconsistency can be accounted for by the organisms’ population differences upon which the percentage resistance was based. The non-marked differences in the overall prevalence of enteric bacteria, and the absence of significant differences in MAR indexes, already indicated abattoir as the source of the housefly-borne enteric bacteria.</p>



<p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; A major objective of the investigation was ascertaining the occurrence of MDR enteric microorganisms in abattoirs located in urban built environments. The results revealed the presence of MDR <em>E. coli, S. enterica, S. dysentariae and K. pneumonia </em>with MAR index.&gt;0.5 in the abattoirs and the surrounding environment. Although the occurrence of MDR bacteria in abattoirs located in Nigeria and other countries have been reported [4, 24-26, 32, 38, 39], this level of MDR bacteria can be seen as not just substantiating these previous reports, but an update in the global trend of antibiotics resistance..This is in line with the need for constant monitoring of trends in antibiotics resistance for the knowledge of public health agencies. This is important in sub-Sahara Africa where antibiotics resistance is increasing but under-reported [40].</p>



<p><em>Implication of findings</em></p>



<p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; The implication of this study outcome is that flies originating from abattoirs can gain access to residential kitchens and deposit MDR bacteria on foods and kitchen utensils which can then spread by cross-contamination. Ill-heath arising from MDR bacteria-contaminated food would be difficult to cure because of limited therapeutic options. The marginal differences in the prevalence of housefly-borne enteric bacteria amongst the abattoirs suggest similar compromised hygienic practices across the abattoirs investigated. &nbsp;This is worrisome hence the need for constant monitoring of hygienic practices in abattoirs. Insistence on the constant use of pesticides for the control of flies by public health agencies can limit the spread of housefly-borne pathogens from abattoirs.</p>



<p><em>Study limitation and future studies</em></p>



<p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; The indoor houseflies were not investigated due to refusal of residents to give their consents. The non-investigation of housefly “nesting” sites near buildings (waste dumpsites, open soak away and septic tanks) for authenticating the source of the flies is a limitation that can be addressed in future studies. The application of social practice theory for interventions in abattoir hygienic practices may be a useful control measure can be explored as indicated in the findings concerning the outdoor environment of makeshift eateries and safety of pushcart foods .[41, 42]</p>



<p><strong>5.0 Conclusion</strong></p>



<p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Houseflies in the urban-based abattoirs were found to be carriers of <em>E. coli,</em> <em>S. enterica, S. dysentariae, </em>and <em>K. pneumonia</em>. These enteric bacteria were isolated from houseflies within the abattoirs and outside at the surrounding buildings’ outdoor environment with a total number of 2008 and 1252 isolates, respectively. The overall prevalence of each enteric bacterial species did not exceed 7.5%. They were all MDR without significant differences in MAR index between those borne on houseflies within and outside the abattoirs. The inference is that the houseflies in the outdoor environment of the buildings emanated from the abattoirs. The spread of MDR enteric bacteria from abattoirs to residential/commercial areas in usually highly populated urban settings should be of concern to public health authorities. These MDR organisms are well known to be associated with gastro-intestinal disease that is challenging to treat. In conclusion, it is important that public health agencies in Nigeria enforce measures for the control of flies in abattoirs and ensure compliance with hygiene standards and regulations. <strong></strong></p>



<p><strong>Conflict of interest</strong></p>



<p>There is no conflict of interest.</p>



<p><strong>Funding</strong></p>



<p>Authors funded the study.</p>



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<p>12. Bustillo-Lecompte, C.,&nbsp;&amp;&nbsp;Mehrvar, M. (2017). Slaughterhouse Wastewater: &nbsp;&nbsp;&nbsp;&nbsp; Treatment, &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Management, and Resource Recovery. In physico-chemical wastewater &nbsp;&nbsp;&nbsp;&nbsp; treatment and resource recovery. pp.&nbsp;153-174. InTech Open. DOI: 10.5772/65499</p>



<p>13. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Okuo, M. &amp;&nbsp;Moses, O. (2015).Effect of thermal and physicochemical treatment on &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; abattoir wastewater – a case study of Ikpoba-Hill Abattoir, <em>Bayero Journal of Pure and &nbsp;&nbsp;&nbsp; Applied Science</em>.&nbsp;<em>8</em>&nbsp;(2),.&nbsp;100-103</p>



<p>14. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ayoade, F. &amp; Olayioye, E.O,(2016). Microbiological assessment of housekeeping practices and environmental impact of selected abattoirs in Lagos and Ogun states of &nbsp;&nbsp;&nbsp;&nbsp; Nigeria. <em>Journal of Applied Biosciences</em>,&nbsp;<em>99,</em> 9363-9372.</p>



<p>15. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Nassiri, H., Zarrin, M., Veys-Behbahani, R., Faramarzi, S. &amp; Nasiri, A. (2015). Isolation &nbsp;&nbsp; and identification of pathogenic filamentous fungi and yeasts from adult housefly &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; (<em>Diptera: Muscidae</em>) captured from the hospital environments in Alivaz city, &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Southwestern Iran.&nbsp;<em>Journal of Medical Entomology,&nbsp; </em><em>52</em>(6), 1351–1356. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; doi:&nbsp;10.1093/jme/tjv140</p>



<p>16. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Davari, B., Kalantar, E., Zahirnia, A. &amp; Moosa-Kazemi, S.H. (2010). Frequency of &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; resistance and susceptible bacteria isolated from houseflies. <em>Iranian Journal of &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Arthropod-Borne Diseases, 4</em>(2), 50-55.</p>



<p>17. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Zurek, L. &amp; Ghosh, A. (2014). Insects represent a link between food animal farms and &nbsp;&nbsp;&nbsp;&nbsp; the urban environment for antibiotic resistance traits,&nbsp;<em>Applied and Environmental &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Microbiology.&nbsp;</em><em>80</em>(12), 3562–3567. doi:&nbsp;10.1128/AEM.00600-14.&nbsp;</p>



<p>18. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Solà-Ginés, M., González-López, J.J., Cameron-Veas, K., Piedra-Carrasco, N., Cerdà-&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Cuéllar, M. &amp; Migura-Garcia, L. (2015). Houseflies (<em>Musca domestica</em>) as vectors for &nbsp; extended-spectrum β-Lactamase-producing&nbsp;<em>Escherichia coli</em>&nbsp;on Spanish Broiler &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Farms.&nbsp;<em>Applied and Environmental Microbiology</em><strong>,</strong><em>81</em>(11), 3604–3611. &nbsp;&nbsp;&nbsp; doi:&nbsp;10.1128/AEM.04252-14.&nbsp;</p>



<p>19. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Hemmatinezhad, B., Ommi,D., Hafshejani, T.T.&amp; Khamesipour, F.(2015). Molecular &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; detection and antimicrobial resistance of&nbsp;<em>Pseudomonas aeruginosa</em>&nbsp;from houseflies &nbsp;&nbsp; (<em>Musca domestica</em>) in Iran. <em>Journal of Venomous Animals and Toxins Including Tropical &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Dis</em>eases; <em>21</em>, 18. doi:&nbsp;10.1186/s40409-015-0021-z.</p>



<p>20.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Doud, C.W &amp; &nbsp;Zurek, L.&nbsp;(2012). <em>Enterococcus faecalis</em>&nbsp;OG1RF:pMV158 survives and</p>



<p>proliferates in the housefly digestive Tract.&nbsp;<em>Journal of Medical Entomology,&nbsp;</em><em>49</em>(1), 150–155. doi:&nbsp;10.1603/ME11167</p>



<p>21. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Bouamama, L., Sorlozano, A., Laglaoui, A., Lebbadi, M., Aarab, A. &amp; Gutierez, J. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; (2010). Antibiotic resistance patterns of bacterial strains isolated from&nbsp;<em>Periplaneta americana</em>&nbsp;and&nbsp;<em>Musca domestica</em>&nbsp;in Tangier; Morocco..&nbsp;<em>Journal of. Infection in &nbsp;&nbsp;&nbsp; Developing. Countries.&nbsp;</em><em>4, </em>194–201. &nbsp; doi:&nbsp;10.3855/jidc.336.&nbsp;</p>



<p>. 22. &nbsp;&nbsp;&nbsp; Zhang, A., Li Y., Guan, Z., Tuo, H., Liu, D., Yang, Y., Xu, C., Lei, C., &amp; Wang, H. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; (2018). Characterization of resistance patterns and detection of apramycin resistance &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; genes in&nbsp;<em>Escherichia coli</em>&nbsp;Isolated from chicken feces and houseflies after apramycin &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; administration.&nbsp;<em>Frontiers in Microbiology.&nbsp;</em> <em>9</em>, 328. doi:&nbsp;10.3389/fmicb.2018.00328</p>



<p>23. Falodun, O.I.&nbsp;&amp; &nbsp;Rabiu, A. G. (2017). Physiochemical and bacteriological quality of an abattoir wastewater discharged into waterbodies in Ibadan, Nigeria and drug resistant profile of isolated Salmonella Species <em>Journal of Microbiology and Biotechnology. Research.,</em>&nbsp;<em>7&nbsp;</em>(4),&nbsp;23-31</p>



<p>-24. &nbsp;&nbsp;&nbsp;&nbsp; Atieno, N. R., Owuor, O. P. &amp; Omwoyo, O. (2013). Isolation of high antibiotic resistant &nbsp; fecal bacteria indicators, Salmonella and Vibrio species from raw abattoirs sewage in &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; peri-urban locations of Nairobi, Kenya.&nbsp;<em>Greener Journal of Biological Sciences.</em> <em>3, </em>172–&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 178. doi:&nbsp;10.15580/gjbs.2013.5.032113539.</p>



<p>25.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Nwanta, J. A., Onunkwo, J. &amp; Ezenduka, E. (2010). Analysis of Nsukka metropolitan &nbsp;&nbsp;&nbsp;&nbsp; abattoir solid waste and its bacterial contents in south eastern Nigeria: public health</p>



<p>Implication,&nbsp;<em>Archives of Environmental &amp; Occupational Health,&nbsp;</em><em>65</em>(1), 21–26. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; doi:&nbsp;10.1080/19338240903390263</p>



<p>26. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Abiade-Paul, C., Kene, I., Chah, K. (2005).&nbsp; Occurrence and antibiogram of Salmonellae in effluent from Nsukka Municipal abattoir, <em>Nigerian Veterinary Journal,&nbsp;</em><em>27</em>(1), 48–53.</p>



<p>27. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Olatoye, I. O., Amosun, E. A. &amp; Ogundipe, G. A. T. (2012). Multidrug-&nbsp;&nbsp;&nbsp;&nbsp; resistant&nbsp;<em>Escherichia coli</em>&nbsp;O157 contamination of beef and chicken in municipal abattoirs &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; of southwest.&nbsp;<em>Nigerian Journal of Natural Sciences,&nbsp;</em><em>10</em>(8), 125–132.</p>



<p>28. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ivbule, M., Miklaševičs, E., Čupāne, L., Bērziņa, L., Bālinš, A. &amp; Valdovska, A. (2017). &nbsp; Presence of methicillin-resistant&nbsp;<em>Staphylococcus aureus</em>&nbsp;in slaughterhouse environment, &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; pigs, carcasses, and workers.&nbsp;<em>Journal of Veterinary Research.</em><em>61</em>(3), 267–277.</p>



<p>doi:&nbsp;10.1515/jvetres-2017-0037.</p>



<p>29.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Bahrndorff, S., de Jonge, N., Skovgård, H. &amp; Nielsen, J. L. (2017). Bacterial &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Communities Associated with Houseflies (<em>Musca domestica L</em>.) Sampled within and &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; between Farms.&nbsp;<em>PLoS ONE.&nbsp;</em><em>12</em>(1), e0169753. doi:&nbsp;10.1371/journal.pone.0169753</p>



<p>30.&nbsp; &nbsp;&nbsp;&nbsp;&nbsp; Ranjbar, R., Izadi, M., Hafshejani, T. T. &amp; Khamesipour,&nbsp;F. (2016). Molecular detection &nbsp; and antimicrobial resistance of <em>Klebsiella pneumoniae </em>from house flies (<em>Musca domestica</em>) in kitchens, farms, hospitals and slaughterhouses. <em>Journal of Infection and &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Public Health</em>, <em>9</em>, 499—505. http://dx.doi.org/10.1016/j.jiph.2015.12.012</p>



<p>31. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Clinical and Laboratory Standards Institute (CLSI) (2012). <em>Performance Standards for &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Antimicrobial Susceptibility Testing; Twenty-Fourth Informational Supplement. </em>CLSI &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Document M100-S22, Wayne, 32(1).</p>



<p>32.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Visciano, P., Schirone, M., Olivastri, A. M. A., Verdecchia, E. &amp; Paparella, A. (2020). &nbsp;&nbsp;&nbsp; Levels of microbial contamination of swine carcasses along the slaughtering process line,&nbsp;<em>Journal of Consumer Protection and Food Safety, </em><em>15</em>(3), 271–276. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; doi:&nbsp;10.1007/s00003-020-01276-z.</p>



<p>33. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Gufe, C., Ndlovu, M. N., Sibanda, Z., Makuvara, Z. &amp; Marumure, J. (2021). &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Prevalence &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; and antimicrobial profile of potentially pathogenic bacteria isolated from &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; abattoir effluents in Bulawayo, Zimbabwe, <em>Scientific African,</em> <em>14</em>: e01059</p>



<p>34. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Geden, C. J., Nayduch, D., Scott, J. G., Burgess, E. R., Gerr A. C., Kaufman, P. E., &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Thomson, J., &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Pickens, V. &amp; Machtinger, E. T. (2021). House Fly (Diptera: Muscidae): &nbsp;&nbsp;&nbsp; Biology, pest &nbsp; status, current management prospects, and research needs, <em>Journal of &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Integrated Pest Management, </em><em>12</em>(1), 39; 1–38 doi: 10.1093/jipm/pmaa021</p>



<p>35. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Lole, M. J.2005. Nuisance flies and landfill activities: an investigation at a</p>



<p>West Midlands landfill site. <em>Waste Management Research</em>, <em>23,</em> 420–428. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Doi:10.1177/0734242X05057694</p>



<p>36. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Winpisinger, K. A., Ferketich, A. K., Berry, R. L. &amp;. Moeschberger, M. L (2005). Spread of <em>Musca domestica </em>(Diptera: muscidae), from two caged layer facilities to neighboring &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; residences in rural Ohio. <em>Journal of Medical Entomolology</em> <em>42,</em> 732–738.</p>



<p>37. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Fried, J. H., Levey, D. J. &amp; Hogsette J. A.<strong> (</strong>2005). Habitat corridors function as both &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; drift fences and movement conduits for dispersing flies. &nbsp;<em>Oecologia</em>, <em>143</em>,: 645–651</p>



<p>38. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Esemu, S. N., Aka, T. K., Kfusi, A. J., Ndip, R. N.&amp; Ndip, L. M. (2022). Multidrug-&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; resistant bacteria and enterobacteriaceae count in abattoir wastes and its receiving waters &nbsp;&nbsp; in Limbe municipality, Cameroon: Public health implications. <em>BioMed Research &nbsp;&nbsp;&nbsp;&nbsp; International,</em> Article ID <em>9977371</em>,&nbsp; &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; <a href="https://doi.org/10.1155/2022/9977371">https://doi.org/10.1155/2022/9977371</a></p>



<p>39. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Umeh, S. I., Udensi, J. U., Nwabueze, E. U., Echeta, M. O., Omeokachie, I. M., N&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; lemolisa. O. R. &amp; Kemka, U. N (2024). Distribution of antibiotics resistant enteric &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; bacteria in Abattoir Waste. <em>Journal of the Learning Sciences</em>, <em>32</em>, 2. TF-JLSER-D-23-&nbsp;&nbsp;&nbsp;&nbsp; 02152</p>



<p>40. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Kariuki, S., Kering, K., Wairimu, C., Onsare, R. &amp; Mbae, C. (2022) Antimicrobial &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; resistance rates and surveillance in sub-Saharan Africa: Where are we now? <em>Infection and &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Drug Resistance,</em> 3589-3609, DOI: 10.2147/IDR.S342753</p>



<p>41. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ejechi, B. O., Akpomie, O. O. &amp; Ejechi, E. O. (2023). Assessment of makeshift eateries ’ &nbsp;&nbsp;&nbsp; outdoor environment for food safety and location of potential intervention points guided &nbsp; by social practice theory. <em>International. Journal.of Environment and Health,</em><em> 11</em>(1): 1-20. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; <strong>DOI</strong>:&nbsp;<a href="https://dx.doi.org/10.1504/IJENVH.2023.135443">10.1504/IJENVH.2023.135443</a>.</p>



<p>42. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ejechi, B. O. and Ejechi, E. O. (2024). Identification of food safety intervention points &nbsp;&nbsp; by Application of Social Practice Theory: case study of pushcart foods, <em>Food Bulletin</em>, &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; <em>3</em>(2), 24-33.&nbsp; <a href="https://doi.org/10.61326/foodb.v3i2.289">https://doi.org/10.61326/foodb.v3i2.289</a></p>
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                                <keyword>non-culturable poultry</keyword>
                                                            
                                <keyword>Nutrient cycling</keyword>
                                                            
                                <keyword>nutrient recycling</keyword>
                                                            
                                <keyword>nutrient retention</keyword>
                                                            
                                <keyword>Oclansorb</keyword>
                                                            
                                <keyword>Oncogenic microbes</keyword>
                                                            
                                <keyword>Oryza sativa</keyword>
                                                            
                                <keyword>Oxygen</keyword>
                                                            
                                <keyword>parasitosis</keyword>
                                                            
                                <keyword>pathogens</keyword>
                                                            
                                <keyword>PBRs</keyword>
                                                            
                                <keyword>Pepper anthracnose</keyword>
                                                            
                                <keyword>personalized nutrition</keyword>
                                                            
                                <keyword>PGPR</keyword>
                                                            
                                <keyword>phage cocktails</keyword>
                                                            
                                <keyword>pharmaceutical cocrystals</keyword>
                                                            
                                <keyword>phosphate-solubilizing fungi</keyword>
                                                            
                                <keyword>Physico-chemical parameters</keyword>
                                                            
                                <keyword>Physicochemical parameters</keyword>
                                                            
                                <keyword>physicochemical properties</keyword>
                                                            
                                <keyword>Phytochemical profiling</keyword>
                                                            
                                <keyword>phytochemicals</keyword>
                                                            
                                <keyword>Phytotherapy</keyword>
                                                            
                                <keyword>plant growth promotion</keyword>
                                                            
                                <keyword>plant immunity</keyword>
                                                            
                                <keyword>plant species</keyword>
                                                            
                                <keyword>Plasmodium falciparum</keyword>
                                                            
                                <keyword>policy frameworks</keyword>
                                                            
                                <keyword>Polymerase chain detection</keyword>
                                                            
                                <keyword>Prebiotics</keyword>
                                                            
                                <keyword>Predictions</keyword>
                                                            
                                <keyword>Pregnant women</keyword>
                                                            
                                <keyword>Probiotics</keyword>
                                                            
                                <keyword>Public Health</keyword>
                                                            
                                <keyword>public health risks</keyword>
                                                            
                                <keyword>questionnaire</keyword>
                                                            
                                <keyword>rainy and dry season</keyword>
                                                            
                                <keyword>Randia aculeata</keyword>
                                                            
                                <keyword>recycling</keyword>
                                                            
                                <keyword>reforestation</keyword>
                                                            
                                <keyword>renewable energy</keyword>
                                                            
                                <keyword>Reproductive aged women</keyword>
                                                            
                                <keyword>resource efficiency</keyword>
                                                            
                                <keyword>resource recovery</keyword>
                                                            
                                <keyword>rhizosphere</keyword>
                                                            
                                <keyword>Risk Factors</keyword>
                                                            
                                <keyword>Salmonella</keyword>
                                                            
                                <keyword>Sand grain size</keyword>
                                                            
                                <keyword>sanitation</keyword>
                                                            
                                <keyword>Sexual Behaviors</keyword>
                                                            
                                <keyword>shelf-life</keyword>
                                                            
                                <keyword>Shigella; Salmonell</keyword>
                                                            
                                <keyword>Silviculture</keyword>
                                                            
                                <keyword>Skin</keyword>
                                                            
                                <keyword>skin penetration</keyword>
                                                            
                                <keyword>Soap</keyword>
                                                            
                                <keyword>Social Well-being</keyword>
                                                            
                                <keyword>socio-environmental factors</keyword>
                                                            
                                <keyword>Soil</keyword>
                                                            
                                <keyword>soil health</keyword>
                                                            
                                <keyword>soil microbes</keyword>
                                                            
                                <keyword>Soil microbiota</keyword>
                                                            
                                <keyword>soil restoration</keyword>
                                                            
                                <keyword>Southern Kaduna</keyword>
                                                            
                                <keyword>Spent oil. Polluted soil</keyword>
                                                            
                                <keyword>Staphylococcus aureus</keyword>
                                                            
                                <keyword>sterilized and unsterilized sand</keyword>
                                                            
                                <keyword>Sub-acute toxicity</keyword>
                                                            
                                <keyword>sustainable agriculture</keyword>
                                                            
                                <keyword>sustainable farming</keyword>
                                                            
                                <keyword>sustainable management</keyword>
                                                            
                                <keyword>sustainable waste management</keyword>
                                                            
                                <keyword>Synbiotics</keyword>
                                                            
                                <keyword>synthetic biology</keyword>
                                                            
                                <keyword>Tamarindus indica</keyword>
                                                            
                                <keyword>Tomato Fusarium wilt</keyword>
                                                            
                                <keyword>topical antifungal therapy</keyword>
                                                            
                                <keyword>Traditional Ecological Knowledge</keyword>
                                                            
                                <keyword>Traditional medicinal plants</keyword>
                                                            
                                <keyword>traditional practices</keyword>
                                                            
                                <keyword>transdermal drug delivery</keyword>
                                                            
                                <keyword>Transferosomes</keyword>
                                                            
                                <keyword>Treatment performance</keyword>
                                                            
                                <keyword>Trichoderma</keyword>
                                                            
                                <keyword>tumorigenesis</keyword>
                                                            
                                <keyword>Type 2 diabetes</keyword>
                                                            
                                <keyword>Urban Green Spaces</keyword>
                                                            
                                <keyword>Urease</keyword>
                                                            
                                <keyword>Urinary tract infections (UTIs)</keyword>
                                                            
                                <keyword>Urine</keyword>
                                                            
                                <keyword>Uropathogens</keyword>
                                                            
                                <keyword>Utilization</keyword>
                                                            
                                <keyword>Vaginal microbiome</keyword>
                                                            
                                <keyword>vancomycin</keyword>
                                                            
                                <keyword>vesicular systems</keyword>
                                                            
                                <keyword>viral oncoproteins</keyword>
                                                            
                                <keyword>Vulvovaginal Candidiasis</keyword>
                                                            
                                <keyword>Wastewater</keyword>
                                                            
                                <keyword>Water</keyword>
                                                            
                                <keyword>water contaminated percolation</keyword>
                                                            
                                <keyword>Water hyacinth</keyword>
                                                            
                                <keyword>Women</keyword>
                                                            
                                <keyword>Xylopia aethiopica</keyword>
                                                            
                                <keyword>Zaria</keyword>
                                                            
                                <keyword>zero waste</keyword>
                                                        
                        </keywords>
                                                                </item>
        </channel>
</rss>